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FDA 510(k)

ESOPHAGEAL INTUBATION DETECTOR ADAPTER - (EID-ADAPTER)

K-Number: K945745 · 1994-12-07

Decision Date1994-12-07
Product CodeBTR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ESOPHAGEAL INTUBATION DETECTOR ADAPTER - (EID-ADAPTER) is the device name listed in this FDA 510(k) record. The listed applicant is Wolfe Tory Medical, Inc.. It received FDA 510(k) clearance on 1994-12-07 under 510(k) number K945745. The device is classified under product code BTR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ESOPHAGEAL INTUBATION DETECTOR ADAPTER - (EID-ADAPTER)?

ESOPHAGEAL INTUBATION DETECTOR ADAPTER - (EID-ADAPTER) is a medical device that received FDA 510(k) clearance on 1994-12-07. The listed applicant is Wolfe Tory Medical, Inc.. The 510(k) number is K945745.

When did ESOPHAGEAL INTUBATION DETECTOR ADAPTER - (EID-ADAPTER) receive FDA 510(k) clearance?

ESOPHAGEAL INTUBATION DETECTOR ADAPTER - (EID-ADAPTER) received FDA 510(k) clearance on 1994-12-07, under 510(k) number K945745.

Who is the listed applicant for ESOPHAGEAL INTUBATION DETECTOR ADAPTER - (EID-ADAPTER)?

The FDA 510(k) record lists Wolfe Tory Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ESOPHAGEAL INTUBATION DETECTOR ADAPTER - (EID-ADAPTER)?

The FDA product code for ESOPHAGEAL INTUBATION DETECTOR ADAPTER - (EID-ADAPTER) is BTR.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Wolfe Tory Medical, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: BTR)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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